NCT Number: NCT00002161
A Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Adefovir Dipivoxil When Added to Standard Antiretroviral Therapy for the Treatment of HIV-Infected Patients With CD4 Cell Counts >= 200/mm3
To evaluate the anti-HIV activity, safety, and tolerance of adefovir dipivoxil ( bis-POM PMEA ) in combination with standard antiretroviral therapy for 48 weeks.
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Notify MeKey information
Conditions
Age range
13 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Univ of Alabama at Birmingham, Birmingham, Alabama, United States
About this study
Patients are randomized to receive either adefovir dipivoxil or placebo daily for 24 weeks, after which all patients will receive open-label drug for an additional 24 weeks. Study drug is administered in combination with a current antiretroviral regimen for the entire 48 weeks. Patients are followed every 4 weeks during the first 24 weeks of study, then every 8 weeks during the last 24 weeks.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients must have:
- HIV infection with HIV RNA titer >= 2500 copies/ml (2.5 KEq/ml) plasma.
- CD4 count >= 200 cells/mm3.
- No new AIDS-defining event within the past 2 months.
- Life expectancy at least 1 year.
- Consent of parent or guardian if less than 18 years old.
- Tolerated antiretroviral therapy for the past 2 months.
NOTE:
- Kaposi's sarcoma is permitted provided patient has not received systemic therapy within the past month.
Exclusion criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Active, serious infections other than HIV that require parenteral antibiotic or antiviral therapy.
- Gastrointestinal malabsorption syndrome or chronic nausea or vomiting that would preclude oral medication.
- Malignancy other than Kaposi's sarcoma or basal cell carcinoma.
Concurrent Medication:
Excluded:
- Immunomodulating agents such as systemic corticosteroids, IL-2, or interferons.
- Isoniazid.
- Rifampin.
- Investigational agents (unless approved by sponsor).
- Systemic chemotherapeutic agents.
Prior Medication:
Excluded:
- Parenteral antibiotic or antiviral therapy for another active, serious infection within the past 2 weeks.
- Immunomodulating agents such as systemic corticosteroids, IL-2, or interferons within the past month.
- Systemic therapy for KS within the past month.
Required:
- Antiretroviral regimen other than study drug.
Required:
- Antiretroviral therapy for at least the past 2 months. Current alcohol or substance abuse that would interfere with compliance.
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Gilead Sciences
Industry
Registry information
Important dates
- First posted
- Aug 31, 2001
- Registry last updated
- Jun 24, 2005
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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